MyVariant.info:
GRCh37
chr11:g.68562335G>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68794867G>C , CM000673.2:g.68794867G>C | GRCh38 |
| NC_000011.9:g.68562335G>C , CM000673.1:g.68562335G>C | GRCh37 |
| NC_000011.8:g.68318911G>C | NCBI36 |
| NG_011801.1:g.52065C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265641.10:c.816C>G MANE Select | ENSP00000265641.4:p.Ala272= | |
| ENST00000265641.9:c.816C>G | ENSP00000265641.4:p.Ala272= | |
| ENST00000376618.6:c.816C>G | ENSP00000365803.2:p.Ala272= | |
| ENST00000538994.1:c.72C>G | ENSP00000454332.1:p.Ala24= | |
| ENST00000539743.5:c.816C>G | ENSP00000446108.1:p.Ala272= | |
| ENST00000540367.5:c.816C>G | ENSP00000439084.1:p.Ala272= | |
| NM_001031847.2:c.816C>G | NP_001027017.1:p.Ala272= | |
| NM_001876.3:c.816C>G | NP_001867.2:p.Ala272= | |
| XM_005273762.1:c.912C>G | XP_005273819.1:p.Ala304= | |
| XM_005273763.1:c.912C>G | XP_005273820.1:p.Ala304= | |
| XM_005273762.3:c.912C>G | XP_005273819.1:p.Ala304= | |
| XM_017017220.1:c.816C>G | XP_016872709.1:p.Ala272= | |
| NM_001876.4:c.816C>G MANE Select | NP_001867.2:p.Ala272= | |
| NM_001031847.3:c.816C>G | NP_001027017.1:p.Ala272= |